Source:http://linkedlifedata.com/resource/pubmed/id/20670037
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
15
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pubmed:dateCreated |
2010-7-30
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pubmed:abstractText |
The first synthesis of the sulfonate analogue of seminolipid, the main sulfoglycolipid in mammalian sperm, is reported. Installation of the sulfonate unit was accomplished by a quite unexplored strategy based on Horner-Wadsworth-Emmons olefination on a 3 '-keto-galactoside, followed by stereoselective double bond reduction.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1520-6904
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
6
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pubmed:volume |
75
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5363-6
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pubmed:meshHeading | |
pubmed:year |
2010
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pubmed:articleTitle |
Synthesis of the sulfonate analogue of seminolipid via Horner-Wadsworth-Emmons olefination.
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pubmed:affiliation |
Dipartimento di Chimica, Biochimica e Biotecnologie per la Medicina, Università di Milano, Via Saldini 50, 20133-Milano, Italy. laura.franchini@unimi.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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